Barely Significant
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Germline variants at SOHLH2 influence multiple myeloma risk.

Blood Cancer J · 2021 · PMC8055668 · PMID 33875642

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nominally significantno p-value reported
Our analysis identified genome-wide significant association signals at 10 loci, and all previously reported MM lead variants were nominally significant with effects in the same direction as in the discovery studies (Supplementary Table 1 ).

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